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Molecular Ecology Resources|April 1, 2023
CRISPR-Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integronEva Sandoval-Quintana, Christina Stangl, Lionel Huang, et al.
Journal of Cardiovascular Translational Research|March 2, 2011
Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsMagdalena Harakalova, Isaäc J Nijman, Jelena Medic, et al.
Nature Protocols|November 5, 2011
Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencingMagdalena Harakalova, Michal Mokry, Barbara Hrdlickova, et al.
American Journal of Human Genetics|March 24, 2015
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspringMirjam S de Pagter, Markus J van Roosmalen, Annette F Baas, et al.
Blood|April 8, 2021
Allele-specific expression of GATA2 due to epigenetic dysregulation in CEBPA double-mutant AMLRoger Mulet-Lazaro, Stanley van Herk, Claudia Erpelinck, et al.
Elife|November 29, 2019
Micronuclei-based model system reveals functional consequences of chromothripsis in human cellsMaja Kneissig, Kristina Keuper, Mirjam S de Pagter, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Discovery of variants unmasked by hemizygous deletionsRon Hochstenbach, Martin Poot, Isaac J Nijman, et al.
Nature Communications|June 7, 2020
Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencingChristina Stangl, Sam de Blank, Ivo Renkens, et al.
NPJ Genomic Medicine|December 10, 2021
Accurate detection of circulating tumor DNA using nanopore consensus sequencingAlessio Marcozzi, Myrthe Jager, Martin Elferink, et al.
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